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NAD(P)H:醌氧化还原酶在 Cyp1a 敲除和 CYP1A 人源化小鼠品系中的表达及其对致癌物马兜铃酸 I 的生物活化作用。

NAD(P)H:quinone oxidoreductase expression in Cyp1a-knockout and CYP1A-humanized mouse lines and its effect on bioactivation of the carcinogen aristolochic acid I.

机构信息

Department of Biochemistry, Faculty of Science, Charles University, Prague, Czech Republic.

出版信息

Toxicol Appl Pharmacol. 2012 Dec 15;265(3):360-7. doi: 10.1016/j.taap.2012.09.004. Epub 2012 Sep 13.

Abstract

Aristolochic acid causes a specific nephropathy (AAN), Balkan endemic nephropathy, and urothelial malignancies. Using Western blotting suitable to determine protein expression, we investigated in several transgenic mouse lines expression of NAD(P)H:quinone oxidoreductase (NQO1)-the most efficient cytosolic enzyme that reductively activates aristolochic acid I (AAI). The mouse tissues used were from previous studies [Arlt et al., Chem. Res. Toxicol. 24 (2011) 1710; Stiborova et al., Toxicol. Sci. 125 (2012) 345], in which the role of microsomal cytochrome P450 (CYP) enzymes in AAI metabolism in vivo had been determined. We found that NQO1 levels in liver, kidney and lung of Cyp1a1⁻/⁻, Cyp1a2⁻/⁻ and Cyp1a1/1a2⁻/⁻ knockout mouse lines, as well as in two CYP1A-humanized mouse lines harboring functional human CYP1A1 and CYP1A2 and lacking the mouse Cyp1a1/1a2 orthologs, differed from NQO1 levels in wild-type mice. NQO1 protein and enzymic activity were induced in hepatic and renal cytosolic fractions isolated from AAI-pretreated mice, compared with those in untreated mice. Furthermore, this increase in hepatic NQO1 enzyme activity was associated with bioactivation of AAI and elevated AAI-DNA adduct levels in ex vivo incubations of cytosolic fractions with DNA and AAI. In conclusion, AAI appears to increase its own metabolic activation by inducing NQO1, thereby enhancing its own genotoxic potential.

摘要

马兜铃酸会导致特定的肾病(AAN)、巴尔干地方性肾病和尿路上皮恶性肿瘤。我们使用适合于确定蛋白质表达的 Western 印迹法,在几个转基因小鼠品系中研究了 NAD(P)H:醌氧化还原酶(NQO1)的表达,NQO1 是还原激活马兜铃酸 I(AAI)的最有效的细胞质酶。我们使用的小鼠组织来自之前的研究[Arlt 等人,Chem. Res. Toxicol. 24(2011)1710;Stiborova 等人,Toxicol. Sci. 125(2012)345],在这些研究中已经确定了微粒体细胞色素 P450(CYP)酶在体内 AAI 代谢中的作用。我们发现,Cyp1a1⁻/⁻、Cyp1a2⁻/⁻和 Cyp1a1/1a2⁻/⁻基因敲除小鼠品系以及两个 CYP1A-人源化小鼠品系(其中包含功能性人 CYP1A1 和 CYP1A2 并且缺乏小鼠 Cyp1a1/1a2 同源物)的肝、肾和肺中的 NQO1 水平与野生型小鼠的 NQO1 水平不同。与未处理的小鼠相比,用 AAI 预处理的小鼠的肝和肾细胞质部分分离出的 NQO1 蛋白和酶活性增加。此外,这种肝 NQO1 酶活性的增加与 AAI 的生物活化以及在用 AAI 和 DNA 进行细胞溶质部分的体外孵育时 DNA 与 AAI 加合物水平的升高有关。总之,AAI 似乎通过诱导 NQO1 来增加自身的代谢活化,从而增强自身的遗传毒性潜力。

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